- Open Access
Maternal immunization with vaccines containing recombinant NetB toxin partially protects progeny chickens from necrotic enteritis
© Keyburn et al.; licensee BioMed Central Ltd. 2013
- Received: 23 September 2013
- Accepted: 29 October 2013
- Published: 13 November 2013
Avian necrotic enteritis is a major economic and welfare issue throughout the global poultry industry and is caused by isolates of Clostridium perfringens that produce NetB toxin. Previously we have shown that birds directly vaccinated with inactivated C. perfringens type A culture supernatant (toxoid) combined with recombinant NetB (rNetB) protein were significantly protected from homologous and heterologous challenge. In the present study the protective effect of maternal immunization was examined. Broiler breeder hens were injected subcutaneously with genetically toxoided rNetB(S254L) alone, C. perfringens type A toxoid and toxoid combined with rNetB(S254L). Vaccination resulted in a strong serum immunoglobulin Y response to NetB in hens immunized with rNetB(S254L) formulations. Anti-NetB antibodies were transferred to the eggs and on into the hatched progeny. Subclinical necrotic enteritis was induced experimentally in the progeny and the occurrence of specific necrotic enteritis lesions evaluated. Birds derived from hens immunized with rNetB(S254L) combined with toxoid and challenged with a homologous strain (EHE-NE18) at either 14 or 21 days post-hatch had significantly lower levels of disease compared to birds from adjuvant only vaccinated hens. In addition, birds from hens immunized with rNetB(S254L) alone were significantly protected when challenged at 14 days post-hatch. These results demonstrate that maternal immunization with a NetB-enhanced toxoid vaccine is a promising method for the control of necrotic enteritis in young broiler chickens.
- Broiler Chicken
- Clostridium Perfringens
- Vaccination Regime
- Necrotic Enteritis
- Broiler Breeder
Necrotic enteritis in chickens has become a major welfare and economic issue for the global poultry industry in recent years . Necrotic enteritis is a complex enteric disease and the causative agent is the Gram-positive, spore-forming bacterium Clostridium perfringens. The primary method of disease control has been to use ionophore anticoccidials or in-feed antibiotics . However, there is global concern that these practices increase the level of bacterial antibiotic resistance . Therefore, it has become increasingly important to develop new interventions for this disease, including the development of vaccines.
Clostridial vaccines in other livestock animals, including cattle, sheep and pigs, have been available for many decades , but an effective vaccine for necrotic enteritis in chickens remains limited with only one vaccine, Netvax®, currently commercially available. This vaccine is based on an alpha-toxin toxoid prepared from a C. perfringens type A strain isolated from a cow (CN 1491 alternately called ATCC 13124) . Other experimental vaccines based on alpha-toxin have been evaluated with variable protective success – and other partially protective C. perfringens antigens have been identified . Recently, several studies have demonstrated that the major toxin produced by pathogenic isolates of avian necrotic enteritis-derived C. perfringens, NetB, is an effective vaccine antigen –. These studies all demonstrated some protective efficacy when NetB was used as a single subunit vaccine, but in addition, it has been shown that rNetB in combination with other cellular and/or secreted antigens gave far greater protection against both homologous and heterologous challenge than any of the components used separately . While these studies demonstrated that NetB based vaccines are effective in protecting birds from disease the delivery of the vaccines by direct vaccination of broiler chicks, is not a practical vaccination regime for the poultry industry. Attempts to vaccinate chickens at one day of age were not successful . Maternal vaccination, by which broiler breeder hens are vaccinated to induce protection in the progeny, is a more efficient method of mass vaccinating large numbers of young birds.
For maternal vaccination to be successful antibodies passed from a vaccinated hen into the egg and the hatched chick must be capable of protecting the chicks from disease. The protective immune response mechanisms acting in parenteral vaccinated birds are not well understood. There are no clear studies that directly address the issue of whether passively transferred immunity can confer protection from disease. Two previously reported studies used C. perfringens toxoid vaccines in maternal vaccination trials and found some protection from necrotic enteritis. In one study  no details are provided regarding the origin of the strains used to produce the toxoids and in the other study  no details are given regarding the source of the toxoid, although a search of product registration documents reveals the strain to be derived from a cow rather than a chicken and not likely to have specific proteins involved in disease, such as NetB and host specific adhesions. The authors of each study suggested that antibodies against alpha-toxin were probably a significant protective factor. We hypothesized that if vaccines based on alpha-toxin, which is non-essential for virulence , could provide some level of protection from disease when maternally-delivered then maternal vaccines based on the essential virulence factor, NetB, should deliver enhanced efficacy.
Previously recombinant NetB was chemically toxoided for use in vaccines . By using a mutated version of NetB with reduced toxic activity the need for chemical toxoiding can be avoided. Other workers  demonstrated that a genetically toxoided version of NetB(W262A) had similar efficacy in vaccination as wild-type recombinant NetB. A structural and mutational analysis of NetB has identified other amino acids that are important for toxic activity . The substitution of serine residue 254 with leucine resulted in defective homo-oligomerization in solution and the mutant protein was no longer haemolytic against chicken and duck red blood cells.
The objective of this present study was to evaluate maternal immunization of vaccines containing NetB for the protection of broiler chickens from necrotic enteritis. We also determined serum IgY antibody responses to NetB in broiler breeder hens after immunization with genetically toxoided rNetB(S254L) alone or in combination with the other C. perfringens proteins present in culture supernatant (toxoid), and the transfer of NetB-specific antibody into progeny. Finally, the progeny were challenged in a disease induction model to evaluate protective immunity against necrotic enteritis lesion formation.
Strain and chemicals
C. perfringens strain EHE-NE18  was the challenge strain in the in vivo necrotic enteritis disease induction models and was used to prepare the toxoid for vaccine formulations.
Animals and housing conditions
Twenty-week-old Ross 308 broiler breeder birds were supplied by Aviagen Australia and managed following the standard guidelines provided by the hatchery. The birds were housed in groups of 12 hens with 2 roosters per group. Immediately prior to the first vaccination blood samples were taken (wing brachial vein) and serum tested for anti-NetB specific IgY to determine whether there had been pre-exposure to this antigen. The hens were vaccinated subcutaneously at 22, 24 and 26 weeks of age. Blood and eggs were collected at 30 weeks (four weeks after the third vaccination) and serum and yolk anti-NetB specific IgY levels measured. Blood was also collected at 40 weeks for anti-NetB IgY measurement.
Fertilized eggs for Challenge Trial 1 were collected throughout week 31 and for Challenge Trial 2 throughout week 41. Eggs were stored at 17 °C throughout the collection period and then transferred to an incubator (Wesfan 924, WA, Australia) and then into a hatcher (Bellsouth, VIC, Australia) at day 18 till hatch.
The toxoid was prepared as previously described . Recombinant NetB(S254L) (rNetB(S254L)) was expressed and purified as previously described . Fifty μg of rNetB(S254L) per dose per bird was used for NetB subunit and NetB supplemented toxoid vaccines. The vaccines were prepared in CSIRO triple adjuvant (60% (v/v) Montanide, 40% (v/v) antigen combined with Quil A, 3 mg/mL, and DEAE-dextran, 30 mg/mL in PBS) to a total volume of 500 μL per dose.
To assess the efficacy of the vaccines in the progeny from immunized hens at two susceptible time points (days 14 to 21), two challenge trials were carried out. In trial 1, fertile eggs were collected five weeks after the third vaccination (31 weeks old hens) and the progeny were challenged at days 21 and 22 followed by necropsy at day 23. In trial 2, fertile eggs were collected 15 weeks after the third vaccination (41 weeks old hens) and birds were challenged one week earlier than in trial 1 (challenged at day 14 and 15 followed by necropsy at day 16). In both trials there were 25 birds per group.
Necrotic enteritis disease induction model
Necrotic enteritis was induced using the C. perfringens in-feed infection model as previously described . Twenty-five chicks for each vaccine group were housed in adjacent, but separate, pens in an animal isolation facility. To assess the disease status of each chicken the birds were euthanized with inhaled carbon dioxide and small intestines (duodenum to ileum) were examined for gross necrotic lesions. Intestinal lesions in the small intestine were scored as before : 0 = no gross lesions; 1 = thin or friable walls; 2 = focal necrosis or ulceration (1–5 foci); 3 = focal necrosis or ulceration (6–15 foci); 4 = focal necrosis or ulceration (16 or more foci); 5 = patches of necrosis 2–3 cm long; 6 = diffuse necrosis typical of field cases. The lesion data were analysed using Kruskal-Wallis one-way ANOVA to determine the likelihood that the vaccinated groups had different levels of disease compared to the adjuvant control group. A blood sample was taken from all birds immediately before challenge and serum was analysed by enzyme-linked immunosorbent assay (ELISA) to measure anti-NetB IgY antibody levels. All animal experiments were assessed, approved and monitored by the Australian Animal Health Laboratory’s Animal Ethics Committee.
Immunoassay detection of antibodies
NetB-specific antibody levels in serum were determined by the end-point dilution method using an ELISA as described previously . IgY antibodies were extracted from egg yolk as previously described , with some modifications. Briefly, the yolk was separated from the albumin and PBS was added at 1:1 ratio. The yolk was then vortexed till it reached a uniformly dispersed solution and was then homogenised for 30 min on a rotating wheel. The solution was centrifuged at 3000 g for 25 min and supernatant containing the IgY collected. The samples were diluted 1:1600 in 1% BSA in PBS and 0.1 mL per well was used in the anti-NetB IgY ELISA.
Antibody transfer from vaccinated hens to progeny
The anti-NetB specific IgY antibodies of chicks hatched from vaccinated hens for trial two were also assessed (14 days of age; Figure 3b). As before, the rNetB(S254L) and Toxoid + rNetB(S254L) groups had significantly higher levels of anti-NetB specific IgY antibodies than the adjuvant group (p < 0.001). However, unlike in the first trial, the toxoid group also had significantly higher levels of anti-NetB specific IgY antibodies compared the adjuvant control birds (p < 0.001). The difference in anti-NetB specific IgY antibody levels between the two trials could be attributed to the earlier time point of collection of the pre-challenge blood samples from the chicks (14 days compared to 21 days).
Transferred antibodies partially protect birds from necrotic enteritis
Summary of trial results
Birds with NE
Average lesion score ± SEMa
Reduction in number of birds with NE (%)
Reduction in group average lesion score (%)
2.6 ± 0.3
2.1 ± 0.2
1.8 ± 0.3
Toxoid + NetB(S254L)
1.2 ± 0.3**
3.0 ± 0.3
1.0 ± 0.3***
1.6 ± 0.3*
Toxoid + NetB(S254L)
0.8 ± 0.3***
In trial two birds were challenged at a younger age; at 14 days post-hatch. Similar to trial one, the toxoid + rNetB(S254L) group had a reduction in the number of birds with lesions (62%, Table 1) and a highly significant reduction (73%) in mean lesion score (p < 0.001) compared to the adjuvant control group (Figure 4b). However, unlike trial one, both the rNetB(S254L) and toxoid alone groups also had fewer birds with lesions (52% and 33% reduction, respectively) and a significant reduction in average lesion scores (p < 0.001 and p < 0.05, respectively) compared to the adjuvant control group.
This is the first study to demonstrate that passive transfer of antibodies from hens vaccinated with NetB-based vaccines can protect progeny from necrotic enteritis at the peak ages of disease susceptibility. It is anticipated that such vaccines would provide a valuable tool for the prevention of necrotic enteritis under field conditions. Previous studies that have investigated passive immunity against necrotic enteritis have been based on vaccines to induce alpha-toxin antibodies [5, 14]. Although alpha-toxin vaccines can clearly provide some level of protection, both when used to directly vaccinate birds and when used for maternal vaccination, the antigen is not an essential virulence factor in the pathogenesis of necrotic enteritis . We hypothesized that using the important necrotic enteritis virulence factor NetB, as either a single subunit vaccine or to enhance a conventional clostridial toxoid vaccine, was likely to provide higher levels of protection than alpha-toxin based vaccines.
The origins of the strains used to produce the maternal toxoid vaccines used in the study reported by Lovland et al.  are not reported and the C. perfringens strain used to generate the toxoid tested in the Crouch et al. study  was isolated from a cow. While this strain produces a large quantity of alpha-toxin  it most likely lacks other proteins involved in pathogenesis in chickens, including NetB. There is evidence that the choice of C. perfringens strain used for toxoid production is likely to influence the degree of protection that can be induced. The most direct evidence for this is the different degrees of efficacy noted by Lanckriet et al.  when comparing toxoids prepared from different strains. The importance of using chicken isolates of C. perfringens for vaccine preparation is supported by the finding of other potential virulence factors genetically linked to netB, a gene found almost exclusively in chicken isolates [20, 21]. The strain used to generate the toxoid in this current study (EHE-NE18) is a strain that was isolated from a chicken with necrotic enteritis and is capable of causing disease under experimental conditions [15, 22]. This strain not only produces alpha-toxin but also produces other proteins involved in disease, including NetB. It is therefore likely to contain a greater range of relevant antigens in toxoid preparations. Although EHE-NE18 does produce NetB, the level of the toxin produced under the in vitro culture conditions used in this current study was generally not sufficient to induce a strong anti-NetB immune response in vaccinated hens compared to the adjuvant control (Figure 1a). The addition of rNetB(S254L) to the toxoid preparation significantly increased the anti-NetB antibody levels in the hens and these antibody levels were also significantly higher in the chicks hatched from vaccinated hens (Figure 3). Transfer of specific antibodies is essential for the protection of young birds, since their immune system is not fully developed, especially the gut-associated lymphoid tissue, the maturation of which is not complete until two weeks of age . The vaccination regime used in this study incorporated three vaccinations across six weeks with the final vaccination occurring when the hens were 26 weeks old. Although we saw no evidence of a drop of egg production in this study (data not shown) this vaccination regime is unlikely be the regime adopted by the poultry industry. Similar to other vaccines used in broiler breeders by the industry, the final vaccine most likely would be administered within the first 18 weeks post hatch to ensure that there is no impact on egg production.
Maternally derived antibodies in the progeny are at maximal levels at the time of hatch and gradually reduce in concentration as the birds mature. The key to the success of a maternal vaccination protocol is to ensure that there are sufficient antibodies circulating at the critical period when the birds are most susceptible to disease. The peak period when necrotic enteritis is a problem in broiler chickens is between 2 to 6 weeks post-hatch , hence we tested vaccine efficacy following challenge within this this critical period. Significant protection was seen in the progeny from hens vaccinated with toxoid plus rNetB(S254L) when challenged with a homologous strain (EHE-NE18) in-feed at day 14 and 21 (Figures 4a and b). Surprisingly, given previous results with directly vaccinated birds , significant protection was observed against in-feed challenge in the birds vaccinated with rNetB(S254L) alone (p < 0.001) and toxoid alone (p < 0.05) when challenged at 14 days (Figure 4b). This result may be due to higher levels of specific antibodies at the time of challenge, although the difference between the serum levels of rNetB(S254L) and toxoid at the time of challenge was not significant (p > 0.1). Even though significant protection was seen in progeny from hens vaccinated with rNetB(S254L) alone and toxoid alone at 14 days, only birds from toxoid plus rNetB(S254L) hens were significantly protected at both 14 and 21 days.
In conclusion, it has been shown that vaccination of broiler breeders with a C. perfringens toxoid preparation derived from a chicken necrotic enteritis strain and enhanced by the addition of non-toxic rNetB(S254L) protein, followed by subsequent transfer of maternal immunity to their progeny, provides significant protection against necrotic enteritis. The ease of delivery indicates that this type of vaccine may be a suitable candidate for use in the poultry industry in the near future.
This research was conducted within the Poultry CRC, established and supported under the Australian Government’s Cooperative Research Centres Program. Support was also provided by the Australian Research Council to the Australian Research Council Centre of Excellence in Structural and Functional Microbial Genomics at Monash University. We thank the Monash University Protein Production Unit for the preparation of purified rNetB(S254L) protein.
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